Welcome to My Personal Page
Thank you so much for reading my post. Lupus is a mysterious chronic autoimmune disease that affects more women and particularly women of color. Joe, our son, currently serves as Vice Chair on the Board of Directors for the National LFA. Our Philly chapter is one of the strongest and longest-running chapters in the U.S. The Haas/Arnold/Seltzer Families stand strong in support of finding a cure for this disease.
It is hard to believe that the Lupus Loop/Walk To End Lupus Now, is only 1 months away. This will be our big 30th and also 20 years after my Cindy, my sister passed! We will once again be virtual, please join us Saturday, October 16, 2021. More details to follow.
Cindy, my sister, was diagnosed with lupus at the age of 20 and lost her battle at the age of 41. My family and I are involved with and support the Lupus Foundation, Philadelphia Tri-State Chapter in its many efforts to raise awareness and funds. Lupus is an autoimmune disease that is still difficult to diagnose, misunderstood and grossly underfunded with no known cause or cure. The money raised helps the Lupus Foundation of America, Philadelphia Tri-State Chapter in their mission to improve the quality of life for all people affected by lupus through programs of research, education, support and advocacy. This is especially supportive for the 45,000+ individuals living with the challenges of lupus in the Philadelphia Tri-State area.
You can make a difference in the continued effort to find the causes of and cure for lupus through locally funded research and advocacy efforts. Click on the Chapter Home link above to find more information on lupus and how you can help us solve the cruel mystery of lupus.
Together, we are making an impact today to fulfill the needs of people affected by lupus, while creating a better future for them and future generations.
Please support me for the Walk to End Lupus Now by making a 100% tax deductible donation! Click "Donate Now" on this page. Thank you!
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